Label
Description
KFPT:PT-149F4KFB CUI has phenotype Hearing abnormality
A Knowledge Graph Assertion from Kids First
KFPT:PT-149F4KFB CUI has phenotype Facial Paresis
KFPT:PT-149F4KFB CUI has phenotype Imaging of brain abnormal
KFPT:PT-149F4KFB CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-149F4KFB CUI has phenotype Limited extraocular movements
KFPT:PT-149F4KFB CUI has phenotype Phenotypic abnormality
KFPT:PT-149F4KFB CUI has phenotype Urogenital Diseases
KFPT:PT-149F4KFB CUI has phenotype Congenital anomaly of face
KFPT:PT-149F4KFB CUI has phenotype Congenital digestive system anomalies
KFPT:PT-149F4KFB CUI has phenotype Cardiovascular Abnormalities